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Ontology Browser
Term:
MYOPATHY, SCAPULOHUMEROPERONEAL (DOID:9002252)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
muscular dystrophy +     
Adult-Onset Muscular Dystrophy with Leukoencephalopathy 
Alpha-B Crystallinopathy with Cataract 
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis 
Bassoe Syndrome 
Becker muscular dystrophy +   
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
congenital muscular dystrophy +   
distal myopathy +   
Duchenne muscular dystrophy +   
Emery-Dreifuss muscular dystrophy +   
facioscapulohumeral muscular dystrophy +   
glycogen storage disease VII  
limb-girdle muscular dystrophy +   
Muscular Dystrophy, Animal +   
Muscular Dystrophy, Barnes Type 
Muscular Dystrophy, Cardiac Type 
Muscular Dystrophy, Mabry Type 
Muscular Dystrophy, Pseudohypertrophic, with Internalized Capillaries 
Myofibrillar Myopathy, ZASP-Related  
Myopathy with Abnormal Lipid Metabolism  
MYOPATHY, SCAPULOHUMEROPERONEAL  
An autosomal dominant muscle disorder characterized by slowly progressive muscle weakness and atrophy affecting both proximal and distal muscles of the upper and lower limbs. (OMIM)
myotonic disease +   
oculopharyngeal muscular dystrophy +   
Oculopharyngodistal Myopathy +   
Progressive Muscular Dystrophy, Pectorodorsal 
scapuloperoneal myopathy +   
Vacuolar Neuromyopathy 

Synonyms
Exact Synonyms: SHPM
Primary IDs: OMIM:616852

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